Canonical Allele Identifier: CA340729907

Gene: IL23R

Linked Data

• dbSNP Id: rs1197056098
• gnomAD v3: 1-67259085-T-C
• gnomAD v4: 1-67259085-T-C
• MyVariant Identifiers: chr1:g.67724768T>C (hg19) ; chr1:g.67259085T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.67259085T>C , CM000663.2:g.67259085T>C	GRCh38
NC_000001.10:g.67724768T>C , CM000663.1:g.67724768T>C	GRCh37
NC_000001.9:g.67497356T>C	NCBI36
NG_011498.1:g.97600T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697149.1:c.1686T>C	ENSP00000513138.1:n.1686T>C
ENST00000697150.1:c.1744T>C	ENSP00000513139.1:n.1744T>C
ENST00000697151.1:c.1677T>C	ENSP00000513140.1:n.1677T>C
ENST00000697164.1:c.1757T>C	ENSP00000513153.1:p.Ile586Thr
ENST00000697165.1:c.1544T>C	ENSP00000513154.1:p.Ile515Thr
ENST00000347310.10:c.1847T>C MANE Select	ENSP00000321345.5:p.Ile616Thr
ENST00000637002.1:c.1238T>C	ENSP00000490340.1:p.Ile413Thr
ENST00000347310.9:c.1847T>C	ENSP00000321345.5:p.Ile616Thr
ENST00000395227.2:c.641T>C	ENSP00000378652.2:p.Ile214Thr
ENST00000425614.3:c.1082T>C	ENSP00000387640.2:p.Ile361Thr
ENST00000473881.2:c.*673T>C	ENSP00000486667.1:n.*673T>C
NM_144701.2:c.1847T>C	NP_653302.2:p.Ile616Thr
XM_005270516.2:c.1085T>C	XP_005270573.1:p.Ile362Thr
XM_011540789.1:c.1937T>C	XP_011539091.1:p.Ile646Thr
XM_011540790.1:c.1847T>C	XP_011539092.1:p.Ile616Thr
XM_011540791.1:c.1847T>C	XP_011539093.1:p.Ile616Thr
XM_011540790.3:c.1847T>C	XP_011539092.1:p.Ile616Thr
XM_011540791.3:c.1847T>C	XP_011539093.1:p.Ile616Thr
XR_001736993.1:n.1927T>C
NM_144701.3:c.1847T>C MANE Select	NP_653302.2:p.Ile616Thr